CAS 3883-43-0: Dichlorodioxolane
Formula:C4H6Cl2O2
InChI:InChI=1/C4H6Cl2O2/c5-3-4(6)8-2-1-7-3/h3-4H,1-2H2/t3-,4-/s2
InChI key:InChIKey=ZOZUXFQYIYUIND-SEFKMRKONA-N
SMILES:Cl[C@H]1[C@H](Cl)OCCO1
Synonyms:- (2R,3R)-2,3-dichloro-1,4-dioxane
- (2S)-2,3-dichloro-1,4-dioxane
- 1,4-Dioxane, 2,3-dichloro-, (2R,3R)-rel-
- 1,4-Dioxane, 2,3-dichloro-, trans-
- p-Dioxane, 2,3-dichloro-, trans-
- rel-(2R,3R)-2,3-Dichloro-1,4-dioxane
- trans-2,3-Dichloro-1,4-dioxane
- trans-2,3-Dichloro-1,4-dioxolane
- trans-2,3-Dichlorodioxane
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Found 5 products.
Trans-2,3-dichloro-1,4-dioxane
CAS:Trans-2,3-dichloro-1,4-dioxanePurity:95%Molecular weight:157.00g/moltrans-2,3-Dichloro-1,4-dioxane
CAS:Formula:C4H6Cl2O2Purity:>96.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:156.99Trans-2,3-dichloro-1,4-dioxane
CAS:Trans-2,3-dichloro-1,4-dioxane is a cyclic compound that belongs to the group of hexacarbonyl compounds. It can be used as a reagent in organic chemistry for the synthesis of thiourea derivatives and other heterocyclic compounds. The trans form is more reactive than the cis form due to its higher electrophilicity. The chemical structure of trans-2,3-dichloro-1,4-dioxane is shown in Figure 1. FIGURE 1: Chemical Structure of Trans-2,3-Dichloro-1,4-Dioxane Trans 2,3 dichloro 1,4 dioxane has been shown to react with tetrahydropyran to generate a variety of products with different chemical structures. This reaction is kinetically controlled and involves an intermediate that has not yet been characterized experimentally or by X ray crystallography. TheFormula:C4H6Cl2O2Purity:Min. 95%Molecular weight:156.99 g/molTRANS-2,3-DICHLORO-1,4-DIOXANE
CAS:Formula:C4H6Cl2O2Purity:96%Color and Shape:SolidMolecular weight:156.9952
